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rs199473308

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473308(A;A)
Make rs199473308(A;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position38551090
GeneSCN5A
is asnp
is mentioned by
dbSNPrs199473308
ebirs199473308
HLIrs199473308
Exacrs199473308
Varsomers199473308
Maprs199473308
PheGenIrs199473308
hapmaprs199473308
1000 genomesrs199473308
hgdprs199473308
ensemblrs199473308
gopubmedrs199473308
geneviewrs199473308
scholarrs199473308
googlers199473308
pharmgkbrs199473308
gwascentralrs199473308
openSNPrs199473308
23andMers199473308
23andMe allrs199473308
SNP Nexus

SNPshotrs199473308
SNPdbers199473308
MSV3drs199473308
GWAS Ctlgrs199473308
Max Magnitude0
ClinVar
Risk rs199473308(A;A)
Alt rs199473308(A;A)
Reference rs199473308(T;T)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene SCN5A
CLNDBN Congenital long QT syndrome
Reversed 1
HGVS NC_000003.11:g.38592581A>T
CLNSRC ClinVar
CLNACC RCV000058759.2,